A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574678



Internal ID20947749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:16116242..16280654hg38UCSC Ensembl
chr8:15973751..16138163hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38164413
hg19164413
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277360
Samples
Known GenesMSR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574678
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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